reference/31885435

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endingPage	421
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pageRange	415-421
publicationName	Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
startingPage	415
bibliographicCitation	Piétu G, Ribba AS, de Paillette L, Chérel G, Lavergne JM, Bahnak BR, Meyer D. Molecular study of von Willebrand disease: identification of potential mutations in patients with type IIA and type IIB. Blood Coagul Fibrinolysis. 1992 Aug;3(4):415–21. PMID: 1420817.
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date	199208
identifier	https://doi.org/10.1097/00001721-199208000-00008 https://doi.org/10.1097/00001721-199203040-00008 https://pubmed.ncbi.nlm.nih.gov/1420817
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Molecular study of von Willebrand disease: identification of potential mutations in patients with type IIA and type IIB
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